NDC11 84126003512
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 84126-0035-12 | 84126-0035 |
| 84126-035-12 | 84126-035 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Old Spice Fiji Dry | ALUMINUM CHLOROHYDRATE | The Procter & Gamble Manufacturing Company | 26b8beaf-a80b-3178-e063-6394a90a2500 | 2025-12-31 | Warnings | 84126-035-12 84126-035 84126003512 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.